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An inactivated quadrivalent influenza virus vaccine (IIV4) is designed for intramuscular administration, specifically formulated to provide protection against four distinct strains of the influenza virus. This vaccine is unique in that it offers active, long-term immunity by exposing the recipient's immune system to modified versions of the influenza viruses. Unlike immune globulins, which provide temporary, passive immunity, vaccines stimulate the immune system to produce its own antibodies, enabling the body to recognize and combat the actual viruses upon future exposure. The manufacturing process of this vaccine involves the use of embryonated chicken eggs, where the influenza virus is cultivated, harvested, and subsequently inactivated using formaldehyde. Following this, the virus is concentrated and purified to ensure safety and efficacy. An adjuvant is incorporated into the vaccine formulation to enhance the immune response, making the vaccine more effective. The quadrivalent formulation specifically targets two different strains of influenza type A and two strains of influenza type B, providing broader protection against circulating influenza viruses. It is important to note that when reporting this vaccine, code 90689 should be used for the 0.25 mL dosage administered intramuscularly, while the actual injection procedure should be reported separately.
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The influenza virus vaccine, quadrivalent (IIV4), is indicated for individuals who require immunization against influenza. This includes:
The administration of the quadrivalent influenza virus vaccine involves several key procedural steps:
Post-procedure care involves advising the patient on potential side effects, which may include soreness at the injection site, low-grade fever, or mild fatigue. Patients should be informed that these reactions are generally mild and resolve within a few days. It is also important to instruct patients to seek medical attention if they experience any severe allergic reactions, such as difficulty breathing or swelling of the face and throat. Additionally, patients should be encouraged to maintain their vaccination records and schedule follow-up vaccinations as recommended for ongoing protection against influenza.
Short Descr | VACC IIV4 NO PRSRV 0.25ML IM | Medium Descr | IIV4 VACC INACTIVATED PRSRV FR 0.25ML DOS IM USE | Long Descr | Influenza virus vaccine, quadrivalent (IIV4), inactivated, adjuvanted, preservative free, 0.25 mL dosage, for intramuscular use | Status Code | Statutory Exclusion (from MPFS, may be paid under other methodologies) | Global Days | XXX - Global Concept Does Not Apply | PC/TC Indicator (26, TC) | 9 - Not Applicable | Multiple Procedures (51) | 9 - Concept does not apply. | Bilateral Surgery (50) | 9 - Concept does not apply. | Physician Supervisions | 09 - Concept does not apply. | Assistant Surgeon (80, 82) | 9 - Concept does not apply. | Co-Surgeons (62) | 9 - Concept does not apply. | Team Surgery (66) | 9 - Concept does not apply. | Diagnostic Imaging Family | 99 - Concept Does Not Apply | APC Status Indicator | Influenza, Pneumococcal Pneumonia, Hepatitis B, and Covid-19 Vaccines; Monoclonal Antibody Therapy Product | ASC Payment Indicator | Influenza vaccine; pneumococcal vaccine. | Type of Service (TOS) | 1 - Medical Care | Berenson-Eggers TOS (BETOS) | none | MUE | 1 |
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2019-07-02 | Changed | FDA approval granted on July 2, 2019. |
2019-01-01 | Added | Added |
2018-06-14 | Added | Code added. |
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